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Tissue transfer

Most tissues transfer the amino acid nitrogen to the liver to dispose of as urea. They, therefore, produce either alanine (from the pyruvate-glucose-alanine cycle, in skeletal muscle, kidney, and intestinal mucosa) or glutamine (skeletal muscle, lungs, neural tissues) or serine (kidney), which are released into the blood and taken up by the liver. [Pg.858]

No growth from spores or tissue transferred. Wrong type of media. Wrong pH Old or dehydrated spores. Scalpel or loop too hot. Sugar in media caramelized. See media preparation. See media preparation Soak in sterilized water for 12-24 hours. Cool tool before contacting spores or tissue. Lower sterilization pressure and temp, to recommended levels. [Pg.219]

Keys et al. (2000) explored five approaches to modeling the pharmacokinetics of di- -butyl phthalate and mono- -butyl phthalate. In a flow-limited version of the model, transfers between blood and tissues are simulated as functions of blood flow, tissue concentrations of di- -butyl phthalate or mono-n-butyl phthalate, and tissue blood partition coefficients, assuming instantaneous partitioning of the compounds between tissue and blood (Ramsey and Anderson 1984). In an enterohepatic circulation version of the model, the transfer of mono-n-butyl phthalate from the liver to the small intestine is represented with a first order rate constant (diffusion-limited) and a time delay constant for the subsequent reabsorption of mono- -butyl phthalate from the small intestine. In a diffusion-limited version of the model, the tissue transfers include a first order rate term (referred to as the permeation constant) that relates the intracellular-to-extracellular concentration gradient to the rates of transfer. This model requires estimates of extracellular tissue volume (ECV) and intracellular volume (ICV) ECV is assumed to be equal to tissue blood volume and ICV is assumed to be equal to the difference between tissue blood volume and... [Pg.73]

In ideal volumes (homogenous infinite size, tissue with Unear isotropic electrical properties), analytical solution can be found as already shown. Even if analytical solutions cannot be found with finite volumes and heterogeneous tissue, transfer functions may be determined from measurements or calculations. The dipole is well-suited for analytical models. [Pg.158]

With short-term biocompatibility confirmed, a trial of long-term implantation in small, controlled wounds was designed. Complex cancer excisions result in deep defects requiring reconstruction using autologous free tissue transfer (free flap reconstruction). The tissue to be transferred is chosen for its composition to meet a reconstructive purpose and commonly is harvested from one of three places the distal forearm on the palmar side (forearm flap—skin, fat, and fascia), the outside of the lower leg... [Pg.649]

J.C. Banis, K. Chunikian, M. Kim, J.M. Gu, G.L. Anderson, S. Kaneko, T. Keelen, J.H. Barker, Prefabricated jejimal free-tissue transfer for tracheal reconstruction an experimental smdy, Plast. Reconstr. Surg. 98 (6) (November 1996) 1046—1051. [Pg.557]

A central biokinetic parameter governing the operation of this compartmental model is the compartmental transfer time. These times cover Pb movement among the various compartments set forth in Figure 9.3. Times are based on plasma Pb. At steady state, the ratios of Pb masses in tissue compartments to plasma Pb masses are equivalent to the ratios of transfer times from tissues to plasma and ECF, and from plasma/ECF to tissues. Transfers are also assumed to be from the central to tissue compartments by a first-order kinetic process (White et al., 1998). [Pg.332]

Combined Revascularization and Free Tissue Transfer Sympathectomy Subintimal Angioplasty Gene Therapy Conclusion References... [Pg.269]

McCarthy WJ, Matsamura JS, Fine, NAet al. Combined arterial reconstruction and free tissue transfer for limb salvage. J Vase Surg 1999 29 814-820. [Pg.289]

Leonard W Winchester, Nee Yin Chou (2006) Monitoring free tissue transfer using laser speckle imaging. SPIE Proc. vol. 6078, Photonic Therapeutics and Diagnostics H San Jose, CA, LISA 2006, pp60780G-l-60780G-8... [Pg.446]


See other pages where Tissue transfer is mentioned: [Pg.301]    [Pg.222]    [Pg.217]    [Pg.232]    [Pg.131]    [Pg.2380]    [Pg.892]    [Pg.222]    [Pg.29]    [Pg.239]    [Pg.156]    [Pg.271]    [Pg.277]    [Pg.277]    [Pg.678]    [Pg.1441]    [Pg.137]    [Pg.100]   


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